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holoprosencephaly 11

holoprosencephaly that has material basis in heterozygous mutation in the CDON gene on chromosome 11q24
MedicalCondition rare_disease Q32144196
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holoprosencephaly 11

Summary

holoprosencephaly 11 is a rare disease[1].

Key Facts

  • holoprosencephaly 11's instance of is recorded as rare disease[2].
  • holoprosencephaly 11's instance of is recorded as class of disease[3].
  • holoprosencephaly 11 is a type of holoprosencephaly[4].
  • holoprosencephaly 11 is a type of genetic disease[5].
  • holoprosencephaly 11 is a type of autosomal dominant disease[6].
  • holoprosencephaly 11's genetic association is recorded as CDON[7].
  • holoprosencephaly 11's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110877[8].
  • holoprosencephaly 11's exact match is recorded as http://identifiers.org/doid/DOID:0110877[9].
  • holoprosencephaly 11's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2162[10].
  • holoprosencephaly 11's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . Disease Ontology. Retrieved . wikidata.org.
  4. [5] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [6] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [7] ↑ . Q905695. Retrieved . wikidata.org.
  7. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  8. [9] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). holoprosencephaly 11. Retrieved May 3, 2026, from https://4ort.xyz/entity/holoprosencephaly-11
MLA “holoprosencephaly 11.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/holoprosencephaly-11.
BibTeX @misc{4ortxyz_holoprosencephaly-11_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{holoprosencephaly 11}}, year = {2026}, url = {https://4ort.xyz/entity/holoprosencephaly-11}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): holoprosencephaly 11 — https://4ort.xyz/entity/holoprosencephaly-11 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/holoprosencephaly-11 · Last refreshed:

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 25d ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Mondo id → MONDO_0013642
    Imported from → —
    Umls cui → C3280215
    Disease ontology id → DOID:0110877
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39943|batch #39943]]: deprecate redundant disease superclasses"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.